Associated Papers
A Rare Cause of Adrenal Insufficiency - Isolated ACTH Deficiency Due to TBX19 Mutation: Long-Term Follow-Up of Two Cases and Review of the Literature.
Kardelen Al AD et al.
Hormone Research in Paediatrics, 2019
A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation.
Unal E et al.
Hormones (athens, Greece), 2018
A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.
Akcan N et al.
Frontiers in Endocrinology, 2017
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